NO20022044L - 1- (cyclic amino) alkylcyclohexane compounds, pharmaceutical compositions thereof and their use as anticonvulsants - Google Patents
1- (cyclic amino) alkylcyclohexane compounds, pharmaceutical compositions thereof and their use as anticonvulsantsInfo
- Publication number
- NO20022044L NO20022044L NO20022044A NO20022044A NO20022044L NO 20022044 L NO20022044 L NO 20022044L NO 20022044 A NO20022044 A NO 20022044A NO 20022044 A NO20022044 A NO 20022044A NO 20022044 L NO20022044 L NO 20022044L
- Authority
- NO
- Norway
- Prior art keywords
- cyclic amino
- compounds
- pharmaceutical compositions
- alleviation
- alkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 239000001961 anticonvulsive agent Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 229940125681 anticonvulsant agent Drugs 0.000 title 1
- 206010010904 Convulsion Diseases 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 229940127351 Uncompetitive NMDA Receptor Antagonists Drugs 0.000 abstract 1
- 230000001773 anti-convulsant effect Effects 0.000 abstract 1
- 230000000573 anti-seizure effect Effects 0.000 abstract 1
- 229960003965 antiepileptics Drugs 0.000 abstract 1
- 230000036461 convulsion Effects 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- -1 optical isomers Chemical class 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000024587 synaptic transmission, glutamatergic Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
- C07D295/033—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4453—Non condensed piperidines, e.g. piperocaine only substituted in position 1, e.g. propipocaine, diperodon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/06—Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Certain 1-cyclic amino-alkylcyclohexanes selected from the group consisting of those of formula (I) wherein R* is -(CH2)n-(CR<6>R<7>)m-NR<8>R<9>; wherein n+m=0,1, or 2; wherein R<1> through R<7> are independently selected from the group consisting of hydrogen and lower-alkyl (1-6c), at least R<1>, R<4>, and R<5> being lower-alkyl, and wherein R<8> and R<9> together represent lower-alkylene -(CH2)x- wherein x is 2 to 5, inclusive, and enantiomers, optical isomers, hydrates, and pharmaceutically acceptable salts thereof, are systemically active uncompetitive NMDA receptor antagonists and are therefore useful in the alleviation of conditions resulting from disturbances of glutamatergic transmission. More importantly, these compounds exhibit outstanding anticonvulsant and anti-seizure activity which is not shared by closely-related noncyclic amino compounds. Pharmaceutical compositions thereof and a method-of-treating conditions which are alleviated by the employment of the same, especially the alleviation of convulsions and seizures, and method for the preparation of the active 1-cyclic amino-alkylcyclohexane compounds involved and the manufacture of medicaments therefrom.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP1999/008317 WO2001032640A1 (en) | 1999-11-01 | 1999-11-01 | 1-cyclic amino-alkylcyclohexane compounds, pharmaceutical compositions thereof, and their use as anticonvulsants |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20022044L true NO20022044L (en) | 2002-04-30 |
| NO20022044D0 NO20022044D0 (en) | 2002-04-30 |
| NO322359B1 NO322359B1 (en) | 2006-09-18 |
Family
ID=8167482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20022044A NO322359B1 (en) | 1999-11-01 | 2002-04-30 | 1- (cyclic amino) alkylcyclohexane compounds, their pharmaceutical preparations and their use as anticonvulsants |
Country Status (24)
| Country | Link |
|---|---|
| EP (1) | EP1228052B1 (en) |
| JP (1) | JP4043236B2 (en) |
| KR (1) | KR100548600B1 (en) |
| CN (1) | CN1264827C (en) |
| AT (1) | ATE361284T1 (en) |
| AU (1) | AU782760B2 (en) |
| CA (1) | CA2389325C (en) |
| CY (1) | CY1106672T1 (en) |
| CZ (1) | CZ20021533A3 (en) |
| DE (1) | DE69936004T2 (en) |
| DK (1) | DK1228052T3 (en) |
| EA (1) | EA005684B1 (en) |
| ES (1) | ES2285870T3 (en) |
| HK (1) | HK1049160B (en) |
| HU (1) | HUP0203275A3 (en) |
| IL (2) | IL149401A0 (en) |
| MX (1) | MXPA02004368A (en) |
| NO (1) | NO322359B1 (en) |
| PL (1) | PL199587B1 (en) |
| PT (1) | PT1228052E (en) |
| SI (1) | SI1228052T1 (en) |
| TW (1) | TWI242547B (en) |
| UA (1) | UA72558C2 (en) |
| WO (1) | WO2001032640A1 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7732162B2 (en) | 2003-05-05 | 2010-06-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases |
| JP5379692B2 (en) | 2006-11-09 | 2013-12-25 | プロビオドルグ エージー | 3-Hydroxy-1,5-dihydro-pyrrol-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcers, cancer and other diseases |
| EP2091948B1 (en) | 2006-11-30 | 2012-04-18 | Probiodrug AG | Novel inhibitors of glutaminyl cyclase |
| EP2481408A3 (en) | 2007-03-01 | 2013-01-09 | Probiodrug AG | New use of glutaminyl cyclase inhibitors |
| EP2142514B1 (en) | 2007-04-18 | 2014-12-24 | Probiodrug AG | Thiourea derivatives as glutaminyl cyclase inhibitors |
| AU2010294214B2 (en) | 2009-09-11 | 2015-05-07 | Vivoryon Therapeutics N.V. | Heterocylcic derivatives as inhibitors of glutaminyl cyclase |
| ES2586231T3 (en) | 2010-03-03 | 2016-10-13 | Probiodrug Ag | Glutaminyl cyclase inhibitors |
| MX2012010470A (en) | 2010-03-10 | 2012-10-09 | Probiodrug Ag | Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5). |
| EP2560953B1 (en) | 2010-04-21 | 2016-01-06 | Probiodrug AG | Inhibitors of glutaminyl cyclase |
| EP2686313B1 (en) | 2011-03-16 | 2016-02-03 | Probiodrug AG | Benzimidazole derivatives as inhibitors of glutaminyl cyclase |
| CN104211663B (en) * | 2014-08-11 | 2017-01-11 | 杭州偶联医药科技有限公司 | (S)-N-methoxy-methyl-2-(pyrrolidine) propionamide and preparation method and application thereof |
| PL3461819T3 (en) | 2017-09-29 | 2020-11-30 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| RU2714135C1 (en) * | 2019-11-22 | 2020-02-12 | Федеральное государственное бюджетное учреждение науки "Институт токсикологии Федерального медико-биологического агентства" | (1-methylpiperidin-4-yl)-2-propyl pentanoate hydrochloride, having cholinolytic and anticonvulsant activity |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3097207A (en) * | 1958-03-06 | 1963-07-09 | Parke Davis & Co | 1-halophenyl and 1-alkoxyphenyl cyclohexylamines |
| CN1136187C (en) * | 1997-06-30 | 2004-01-28 | 莫茨股份公司 | 1-amino-alkylcyclohexane NMDA receptor antagonists |
-
1999
- 1999-01-11 UA UA2002054475A patent/UA72558C2/en unknown
- 1999-11-01 MX MXPA02004368A patent/MXPA02004368A/en not_active IP Right Cessation
- 1999-11-01 CN CNB998169900A patent/CN1264827C/en not_active Expired - Fee Related
- 1999-11-01 DE DE69936004T patent/DE69936004T2/en not_active Expired - Fee Related
- 1999-11-01 DK DK99974146T patent/DK1228052T3/en active
- 1999-11-01 WO PCT/EP1999/008317 patent/WO2001032640A1/en active IP Right Grant
- 1999-11-01 KR KR1020027005621A patent/KR100548600B1/en not_active IP Right Cessation
- 1999-11-01 SI SI9930972T patent/SI1228052T1/en unknown
- 1999-11-01 HU HU0203275A patent/HUP0203275A3/en unknown
- 1999-11-01 EA EA200200522A patent/EA005684B1/en not_active IP Right Cessation
- 1999-11-01 AU AU11585/00A patent/AU782760B2/en not_active Ceased
- 1999-11-01 ES ES99974146T patent/ES2285870T3/en not_active Expired - Lifetime
- 1999-11-01 CA CA002389325A patent/CA2389325C/en not_active Expired - Fee Related
- 1999-11-01 PL PL354519A patent/PL199587B1/en not_active IP Right Cessation
- 1999-11-01 PT PT99974146T patent/PT1228052E/en unknown
- 1999-11-01 EP EP99974146A patent/EP1228052B1/en not_active Expired - Lifetime
- 1999-11-01 CZ CZ20021533A patent/CZ20021533A3/en unknown
- 1999-11-01 AT AT99974146T patent/ATE361284T1/en not_active IP Right Cessation
- 1999-11-01 IL IL14940199A patent/IL149401A0/en active IP Right Grant
- 1999-11-01 JP JP2001534791A patent/JP4043236B2/en not_active Expired - Fee Related
- 1999-11-15 TW TW088119884A patent/TWI242547B/en not_active IP Right Cessation
-
2002
- 2002-04-29 IL IL149401A patent/IL149401A/en not_active IP Right Cessation
- 2002-04-30 NO NO20022044A patent/NO322359B1/en not_active IP Right Cessation
-
2003
- 2003-02-18 HK HK03101158.3A patent/HK1049160B/en not_active IP Right Cessation
-
2007
- 2007-06-21 CY CY20071100831T patent/CY1106672T1/en unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |